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Biotin-PEG(3)-NH2
Nom chimique: N-[2-[2-[2-(2-Aminoethoxy)ethoxy]ethoxy]ethyl]biotinamide // Synonymes: Biotin-PEG3-Amine, N-Biotinyl-3,6,9-trioxaundecane-1,11-diamine, Amine-PEG3-Biotin, Biotinyl-PEG3-NH2,N-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]im idazol-4-yl)pentanamide
- n° Art.:RL-4210
- n° CAS:359860-27-8
- Formule:C18H34N4O5S
- Storage temperature:-20°C
- Masse moléculaire:418,22 g/mol
- Pureté:min.97%
from 84,00 €
description
Biotinylation reagent.
references
Serum apolipoprotein A-I potentiates the therapeutic efficacy of lysocin E against Staphylococcus aureus; H. Hamamoto, S. Panthee, A. Paudel, K. Ishii, J. Yasukawa, J. Su, A. Miyashita, H. Itoh, K. Tokumoto, M. Inoue, K. Sekimizu; Nat Commun 2021, 12: 6364. https://doi.org/10.1038/s41467-021-26702-0
Chiral Quantum Metamaterial for Hypersensitive Biomolecule Detection; M. Hajji, M. Cariello, C. Gilroy, M. Kartau, C. D. Syme, A. Karimullah, N. Gadegaard, A. Malfait, P. Woisel, G. Cooke, W. J. Peveler, M. Kadodwala; ACS Nano 2021; 15(12): 19905-19916. https://doi.org/10.1021/acsnano.1c07408
Dissecting the molecular determinants of clinical PARP1 inhibitor selectivity for tankyrase1; K. Ryan, B. Bolaòos, M. Smith, P. B. Palde, P. D. Cuenca, T. L. VanArsdale, S. Niessen, L. Zhang, D. Behenna, M. A. Ornelas, K. T. Tran, S. Kaiser, L. Lum, A. Stewart, K. S. Gajiwala; J. Biol. Chem. 2021; 296: 100251. https://doi.org/10.1074/jbc.RA120.016573
Biotinylated Phosphorus Dendrimers as Control Line in Nucleic Acid Lateral Flow Tests; L. Vidal, A. B. Aissa, J. Salabert, J. J. Jara, A. Vallribera, M. I. Pividori, R. M. Sebastián; Biomacromolecules 2020; 21 (3): 1315–1323. https://doi.org/10.1021/acs.biomac.0c00161
Bioorthogonal Ligation and Cleavage by Reactions of Chloroquinoxalines with ortho-Dithiophenols; Y. Li, Z. Lou, H. Li, H. Yang, Y. Zhao, H. Fu; Angew. Chem. Int. Ed. 2020; 59(9): 3671-367. https://doi.org/10.1002/anie.201913620
COMBINES-CID: An Efficient Method for De Novo Engineering of Highly Specific Chemically Induced Protein Dimerization Systems; S. Kang, K. Davidsen, L. Gomez-Castillo, H. Jiang, X. Fu, Z. Li, Y. Liang, M. Jahn, M. Moussa, F. DiMaio, L. Gu; J. Am. Chem. Soc. 2019, 141(28): 10948–10952. https://doi.org/10.1021/jacs.9b03522
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